Could a virtual board help doctors tackle prostate cancer genetics?
NCT ID NCT04789018
First seen Jun 25, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study looks at whether a web-based virtual genetics board helps doctors discuss and manage prostate cancer genetics. About 118 healthcare providers, including oncologists and genetic counselors, will use the board and then give feedback through surveys and interviews. The goal is to see if the tool is useful and easy to use, not to directly treat patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Educational intervention (virtual genetics board)
- What this could lead to
- If successful, this could lead to a tool that helps doctors better use genetic information to treat and screen for prostate cancer.
- What could go wrong
- This is a small, early-stage study focused on provider opinions, not patient outcomes. The tool may not prove useful or practical in real-world settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
118 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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Dec 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Non-genetic providers who perform prostate cancer (PCA) genetic testing for men in their practices (medical oncologists, radiation oncologists, urologists, primary care providers, mid-level providers)
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Individuals must meet one of the following inclusion criteria in order to be eligible to participate in the study: * Healthcare providers (medical oncologists, radiation oncologists, urologists, primary care providers, mid-level providers) who evaluate, manage, or treat men with prostate cancer or screen men for prostate cancer. * Providers who perform prostate cancer genetic testing for men (genetic counselors or healthcare providers) * Scientists and researchers * Advocacy or patient stakeholder organization members Exclusion Criteria: • Non-medical providers
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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Other studies related to the condition(s) this trial covers.
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